Class Class II

ArtFX Spinal Fixation System (K212220)

K212220 2023-04-20 Traditional
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Description

ArtFX Spinal Fixation System by Artfx Medical, LLC — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK212220
Clearance Date2023-04-20
Clearance TypeTraditional
Product CodeNKB
Regulation Number888.3070

Categories

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